ES2143238T3 - DERIVATIVES OF 1- (PIPERIDINIL SUBSTITUTED IN POSITIONS 1,2) -PIPERAZINES SUBSTITUTED IN POSITION 4. - Google Patents
DERIVATIVES OF 1- (PIPERIDINIL SUBSTITUTED IN POSITIONS 1,2) -PIPERAZINES SUBSTITUTED IN POSITION 4.Info
- Publication number
- ES2143238T3 ES2143238T3 ES96937248T ES96937248T ES2143238T3 ES 2143238 T3 ES2143238 T3 ES 2143238T3 ES 96937248 T ES96937248 T ES 96937248T ES 96937248 T ES96937248 T ES 96937248T ES 2143238 T3 ES2143238 T3 ES 2143238T3
- Authority
- ES
- Spain
- Prior art keywords
- het
- alkyl
- rent
- substituted
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 2
- 239000005557 antagonist Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Hospice & Palliative Care (AREA)
- Otolaryngology (AREA)
- Anesthesiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
ESTA INVENCION SE RELACIONA CON COMPUESTOS DE FORMULA (I), LAS FORMAS N-OXIDO, LAS SALES DE ADICION FARMACEUTICAMENTE ACEPTABLES Y SUS FORMAS ESTEROISOMERICAS, EN LAS QUE N ES 0, 1 O 2; M ES 1 O 2, CON TAL QUE, SI M ES 2, ENTONCES N ES 1; P ES 1 O 2; = Q ES = O O = NR 3 ; X ES UN ENLACE COVALENTE O UN RADICAL BIVALENTE DE FORMULA O-, -S-, -NR 3 -; R 1 ES AR 1 , AR 1 , AR 1 C 1-6 ALQUILO O DI(AR 1 )C 1-6 ALQUILO, EN DONDE CADA GRUPO C 16 ALQUILO ES OPCIONALMENTE SUSTITUIDO CON HIDROXI, C 14 ALQUILOXI, OXO O UN SUBSTITUYENTE OXO CETALIZADO; R 2 ES AR 2 , AR SUP,1 C 1-6 ALQUILO, HET 1 O HET 1 C 1-6 ALQ UILO; R 3 ES HIDROGENO O UN ALQUILO C 1-6 ; L ES HIDROGENO; AR 3 ; C 1-6 ALQUILO; C 1-6 ALQUILO SUSTITU IDO CON 1 O 2 SUBSTITUYENTES SELECCIONADOS DE UN GRUPO DE HIDROXI, C 1-6 ALQUILOXI, AR 3 , AR 3 C 1-6 ALQUIL OXI Y HET 2 ; C 36 ALQUENILO; AR 3 C 3-6 ALQUENILO; DI(AR 3 )C 36 ALQUENILO O UN RADICAL DE FORMULA (A-1), (A-2), (A-3), (A-4) O (A-5); AR 1 , AR 2 , AR SUP,3 SON TODOS FENILO O FENILOSUSTITUIDO; HET 1 Y HET S UP,2 SON HETEROCICLOS MONOCICLICOS O BICICLICOS; ESTOS COMPUESTOS SON ANTAGONISTAS DE LA SUSTANCIA P; SE DESCRIBE SU PREPARACION, COMPOSICIONES QUE LOS CONTIENEN Y SU USO COMO MEDICAMENTOS.THIS INVENTION IS RELATED TO COMPOUNDS OF FORMULA (I), N-OXIDE FORMS, PHARMACEUTICALLY ACCEPTABLE ADDITIONAL SALTS AND THEIR STEROISOMERIC FORMS, IN WHICH N IS 0, 1 OR 2; M IS 1 OR 2, SO IF M IS 2, THEN N IS 1; P ES 1 O 2; = Q ES = O O = NR 3; X IS A COVALENT LINK OR A BIVALENT RADICAL OF FORMULA O-, -S-, -NR 3 -; R 1 IS AR 1, AR 1, AR 1 C 1-6 RENT OR DI (AR 1) C 1-6 RENT, WHERE EACH GROUP C 16 RENT IS OPTIONALLY SUBSTITUTED WITH HYDROXY, C 14 ALKYL OXY, OX OR A SUBSTITUTE OXO CETALLIZED; R 2 ES AR 2, AR SUP, 1 C 1-6 ALKYL, HET 1 OR HET 1 C 1-6 ALK UILO; R 3 IS HYDROGEN OR A C 1-6 ALKYL; L IS HYDROGEN; AR 3; C 1-6 RENT; C 1-6 ALKYL SUBSTITUTE IDO WITH 1 OR 2 SELECTED SUBSTITUTES FROM A GROUP OF HYDROXY, C 1-6 ALKYLLOX, AR 3, AR 3 C 1-6 ALKYL OXI AND HET 2; C 36 ALKYLENE; AR 3 C 3-6 ALKYNYLL; DI (AR 3) C 36 ALKYLLY OR A RADICAL OF FORMULA (A-1), (A-2), (A-3), (A-4) O (A-5); AR 1, AR 2, AR SUP, 3 ARE ALL PHENYL OR SUBSTITUTE PHENYL; HET 1 AND HET S UP, 2 ARE MONOCYCLE OR BICYCLE HETEROCICLES; THESE COMPOUNDS ARE ANTAGONISTS OF THE SUBSTANCE P; THEIR PREPARATION, COMPOSITIONS CONTAINING THEM AND THEIR USE AS MEDICINES ARE DESCRIBED.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP95202929 | 1995-10-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2143238T3 true ES2143238T3 (en) | 2000-05-01 |
Family
ID=8220780
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES96937248T Expired - Lifetime ES2143238T3 (en) | 1995-10-30 | 1996-10-25 | DERIVATIVES OF 1- (PIPERIDINIL SUBSTITUTED IN POSITIONS 1,2) -PIPERAZINES SUBSTITUTED IN POSITION 4. |
Country Status (31)
| Country | Link |
|---|---|
| US (3) | US6197772B1 (en) |
| EP (1) | EP0862566B1 (en) |
| JP (1) | JP3073238B2 (en) |
| KR (1) | KR100407067B1 (en) |
| CN (2) | CN100415716C (en) |
| AR (1) | AR004698A1 (en) |
| AT (1) | ATE188691T1 (en) |
| AU (1) | AU704155B2 (en) |
| BR (1) | BR9611184B8 (en) |
| CA (1) | CA2234096C (en) |
| CY (1) | CY2177B1 (en) |
| CZ (1) | CZ291794B6 (en) |
| DE (1) | DE69606196T2 (en) |
| DK (1) | DK0862566T3 (en) |
| EA (1) | EA000909B1 (en) |
| ES (1) | ES2143238T3 (en) |
| GR (1) | GR3033154T3 (en) |
| HR (1) | HRP960507B1 (en) |
| HU (1) | HU227341B1 (en) |
| IL (1) | IL123962A (en) |
| MX (1) | MX9803407A (en) |
| MY (1) | MY116575A (en) |
| NO (1) | NO310232B1 (en) |
| NZ (1) | NZ321575A (en) |
| PL (1) | PL185029B1 (en) |
| PT (1) | PT862566E (en) |
| SI (1) | SI0862566T1 (en) |
| TR (1) | TR199800756T2 (en) |
| TW (1) | TW460473B (en) |
| WO (1) | WO1997016440A1 (en) |
| ZA (1) | ZA969090B (en) |
Families Citing this family (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ321575A (en) * | 1995-10-30 | 1999-05-28 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4- substituted piperazine derivatives |
| TW382017B (en) | 1995-12-27 | 2000-02-11 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4-(fused imidazole)-piperidine derivatives |
| TW429256B (en) * | 1995-12-27 | 2001-04-11 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4-(benzimidazolyl- and imidazopyridinyl)-piperidine derivatives |
| TW531537B (en) | 1995-12-27 | 2003-05-11 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4-substituted piperidine derivatives |
| AU2307899A (en) * | 1997-12-23 | 1999-07-12 | Alcon Laboratories, Inc. | Muscarinic agents and use thereof to treat glaucoma, myopia and various other conditions |
| US6689765B2 (en) | 1999-05-04 | 2004-02-10 | Schering Corporation | Piperazine derivatives useful as CCR5 antagonists |
| US6391865B1 (en) | 1999-05-04 | 2002-05-21 | Schering Corporation | Piperazine derivatives useful as CCR5 antagonists |
| USRE39921E1 (en) | 1999-10-07 | 2007-11-13 | Smithkline Beecham Corporation | Chemical compounds |
| GB9923748D0 (en) | 1999-10-07 | 1999-12-08 | Glaxo Group Ltd | Chemical compounds |
| WO2001030348A1 (en) * | 1999-10-25 | 2001-05-03 | Janssen Pharmaceutica N.V. | Use of substance p antagonists for influencing the circadian timing system |
| GB0025354D0 (en) * | 2000-10-17 | 2000-11-29 | Glaxo Group Ltd | Chemical compounds |
| ES2342942T3 (en) | 2001-03-29 | 2010-07-19 | Schering Corporation | CCR5 ANTAGONISTS USEFUL FOR THE TREATMENT OF AIDS. |
| GB0108594D0 (en) * | 2001-04-05 | 2001-05-23 | Glaxo Group Ltd | Chemical compounds |
| GB0203022D0 (en) | 2002-02-08 | 2002-03-27 | Glaxo Group Ltd | Chemical compounds |
| WO2003066589A1 (en) * | 2002-02-08 | 2003-08-14 | Glaxo Group Limited | Piperidylcarboxamide derivatives and their use in the treatment of tachykinim-mediated diseases |
| GB0203020D0 (en) * | 2002-02-08 | 2002-03-27 | Glaxo Group Ltd | Chemical compounds |
| CA2487141C (en) | 2002-06-24 | 2011-08-02 | Janssen Pharmaceutica N.V. | Process for the production of n-(2,6-dimethyl-phenyl)-2-piperazin-1-yl-acetamide |
| UA81918C2 (en) * | 2002-10-08 | 2008-02-25 | Янссен Фармацевтика Н.В. | Normal;heading 1;heading 2;SUBSTITUTED 1,4-DI-PIPERIDIN-4-YL-PIPERAZINE DERIVATIVES AND THEIR USE AS NEUROKININ ANTAGONISTS |
| WO2004056772A1 (en) * | 2002-12-23 | 2004-07-08 | Janssen Pharmaceutica N.V. | Substituted 1,4-di-piperidin-4-yl-piperazine derivatives and their use as tachykinin antagonists |
| MY141736A (en) * | 2002-10-08 | 2010-06-15 | Elanco Animal Health Ireland | Substituted 1,4-di-piperidin-4-yi-piperazine derivatives and their use as neurokinin antagonists |
| US7582761B2 (en) * | 2002-10-17 | 2009-09-01 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| JO2485B1 (en) * | 2002-12-23 | 2009-01-20 | شركة جانسين فارماسوتيكا ان. في | Substituted 1- Piperidin- 3- Yl- 4- Piperidin- 4- Yl- Piperazine Derivatives and their Use as Neurokinin Antagonists |
| EP1578744B1 (en) | 2002-12-23 | 2008-07-09 | Janssen Pharmaceutica N.V. | Substituted 4-(4-piperidin-4-yl-piperazin-1-yl)-azepane derivatives and their use as neurokinin antagonists |
| JO2696B1 (en) | 2002-12-23 | 2013-03-03 | شركة جانسين فارماسوتيكا ان. في | Substituted 1-piperidin-4-yl-4-pyrrolidin-3-yl-piperazine derivatives and their use as neurokinin antagonists |
| JP4660199B2 (en) | 2002-12-23 | 2011-03-30 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Substituted 1-piperidin-4-yl-4-azetidin-3-yl-piperazine derivatives and their use as neurokinin antagonists |
| DE602004013772D1 (en) * | 2003-06-10 | 2008-06-26 | Janssen Pharmaceutica Nv | Combination of opioids and a piperazine derivative for the treatment of pain |
| JP2006527236A (en) * | 2003-06-10 | 2006-11-30 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Substituted 1,4-di-piperidin-4-yl-piperazine derivatives in combination with opioid analgesics and their use for the treatment of pain and side effects associated with opioid based treatments |
| UY28538A1 (en) * | 2003-09-26 | 2005-04-29 | Vertex Pharma | PHENYL-PIPERAZINE DERIVATIVES AS MUSCARINIC RECEPTORS MODULATORS |
| JO2676B1 (en) * | 2004-04-06 | 2012-06-17 | جانسين فارماسوتيكا ان. في | Substituted diaza-spiro-(4,5)-Decane derivatives and their use as neurokinin antagonists |
| JO2527B1 (en) * | 2004-04-06 | 2010-03-17 | شركة جانسين فارماسوتيكا ان. في | Substiuted diaza-spiro-(5,5)-Deacan derivatives and there use as neurokinin antagonist |
| JO2525B1 (en) * | 2004-04-08 | 2010-03-17 | شركة جانسين فارماسوتيكا ان. في | Substiuted 4-alkyl-and 4-alkanoyl piperidine derivatives and there use as neurokinin antagonist |
| ES2431524T3 (en) | 2004-04-13 | 2013-11-26 | Incyte Corporation | Piperazinylpiperidine derivatives as chemokine receptor antagonists |
| WO2005123081A2 (en) * | 2004-06-22 | 2005-12-29 | Janssen Pharmaceutica N.V. | (2-benzyl-4-{4-[1-(tetrahydrofuran-3-carbonyl)-pyrrolidin-3-yl]-piperazin-1-yl}-piperidin-1-yl)-(3,5-trifluoromethyl-phenyl))-methanone for the treatment of schizophrenia |
| US20060024481A1 (en) * | 2004-07-29 | 2006-02-02 | Eastman Kodak Company | Jet printing of patterned metal |
| CA2576166C (en) | 2004-08-19 | 2018-02-20 | Monsanto Technology Llc | Glyphosate salt herbicidal composition |
| WO2006071958A1 (en) * | 2004-12-29 | 2006-07-06 | Millennium Pharmaceuticals, Inc. | Compounds useful as chemokine receptor antagonists |
| NZ556628A (en) | 2005-03-08 | 2009-09-25 | Janssen Pharmaceutica Nv | Diaza-spiro-[4.4]-nonane derivatives as neurokinin (NK1) antagonists |
| CN101190330A (en) | 2006-11-30 | 2008-06-04 | 深圳市鼎兴生物医药技术开发有限公司 | Application of cholinesterase in antagonizing tachykinin drugs |
| WO2008090114A1 (en) | 2007-01-24 | 2008-07-31 | Glaxo Group Limited | Pharmaceutical compositions comprising 2-methoxy-5- (5-trifluoromethyl-tetrazol-i-yl-benzyl) - (2s-phenyl-piperidin-3s-yl-) |
| WO2010081851A1 (en) | 2009-01-14 | 2010-07-22 | Genoscience Pharma | Piperidin-4-ylpiperazine compounds for the treatment of hcv infection |
| GB201106817D0 (en) | 2011-04-21 | 2011-06-01 | Astex Therapeutics Ltd | New compound |
| GB201218850D0 (en) | 2012-10-19 | 2012-12-05 | Astex Therapeutics Ltd | Bicyclic heterocycle compounds and their uses in therapy |
| GB201218864D0 (en) | 2012-10-19 | 2012-12-05 | Astex Therapeutics Ltd | Bicyclic heterocycle compounds and their uses in therapy |
| US9980973B2 (en) | 2012-10-19 | 2018-05-29 | Astex Therapeutics Limited | Bicyclic heterocycle compounds and their uses in therapy |
| GB201218862D0 (en) | 2012-10-19 | 2012-12-05 | Astex Therapeutics Ltd | Bicyclic heterocycle compounds and their uses in therapy |
| CN111557432B (en) | 2013-02-08 | 2023-08-04 | 通用磨坊公司 | Low sodium food |
| LT3083616T (en) | 2013-12-20 | 2021-09-10 | Astex Therapeutics Limited | BICYCLIC HETEROCYCL COMPOUNDS AND THEIR USE IN THERAPY |
| MX371178B (en) * | 2016-01-08 | 2020-01-21 | Nerre Therapeutics Ltd | ORVEPITANT FOR THE TREATMENT OF CHRONIC COUGH. |
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| FR2676055B1 (en) * | 1991-05-03 | 1993-09-03 | Sanofi Elf | AMINO POLYCYCLIC COMPOUNDS AND THEIR ENANTIOMERS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
| MY110227A (en) * | 1991-08-12 | 1998-03-31 | Ciba Geigy Ag | 1-acylpiperindine compounds. |
| CN1042335C (en) * | 1993-01-03 | 1999-03-03 | 诺瓦提斯公司 | 1-acylpiperidine compounds |
| ATE157349T1 (en) * | 1993-05-12 | 1997-09-15 | Heumann Pharma Gmbh & Co | STABLE AND CRYSTALLINE FORM OF BEZAFIBRATE |
| GB9310066D0 (en) * | 1993-05-17 | 1993-06-30 | Zeneca Ltd | Alkyl substituted heterocycles |
| WO1995011895A1 (en) * | 1993-10-26 | 1995-05-04 | Ciba-Geigy Ag | N-benzoyl-4-oxy/thio-2-substituted piperidines as substance-p receptor antagonists |
| IL111730A (en) * | 1993-11-29 | 1998-12-06 | Fujisawa Pharmaceutical Co | Piperazine derivatives processes for the preparation thereof and pharmaceutical compositions containing the same |
| KR100254666B1 (en) * | 1994-07-15 | 2000-05-01 | 이치로 키타사토 | Novel compounds with platelet aggregation inhibitory action |
| CA2198382A1 (en) * | 1994-09-30 | 1996-04-11 | Novartis Ag | 1-acyl-4-aliphatylaminopiperidine compounds |
| NZ321575A (en) * | 1995-10-30 | 1999-05-28 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4- substituted piperazine derivatives |
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1994
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1998
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2000
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2001
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